Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.47 (G)

Chromosome 11:108368901 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs664329, rs3202133

This variation has 10 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2583 individual genotypes and is mentioned in 2 citations.

Variation displays